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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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cognitive decline

Kufor-Rakeb Syndrome

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Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy, Childhood-Onset

Coats Plus Syndrome

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Premature telomere shortening results from mutations in the gene CTC1 which allows chromosomes to degrade prematurely and shorten the time of cell divisions.

Spastic Paraplegia 46

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Niemann-Pick Disease, Type C2

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College of Medicine
Department of Ophthalmology and Vision Science
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